galaxyproject / galaxy-beta1Links
Galaxy Github repository BETA 1. May be destroyed and recreated if post-conversion problems are found (but post-conversion commits on this repo will be reapplied to any recreations). Scary disclaimer aside, so far so good! Full details:
☆12Updated 10 years ago
Alternatives and similar repositories for galaxy-beta1
Users that are interested in galaxy-beta1 are comparing it to the libraries listed below
Sorting:
- An easy-to-use way for running Galaxy workflows.☆20Updated 5 years ago
- FLS Galaxy tools and tool-wrappers for in-house and third-party bioinformatic applications.☆14Updated last year
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 5 months ago
- cache packages permanently☆14Updated 11 months ago
- ☆12Updated 2 years ago
- A fast tool to convert BioJS components into Galaxy visualization plugins.☆14Updated 4 years ago
- Simon's Data Club - Reference data for Galaxy servers☆10Updated last year
- Open-source opinionated Galaxy-based framework for microbiota analysis☆14Updated 4 years ago
- vcf file manipulation☆21Updated 9 years ago
- Awesome resources related to Galaxy project☆12Updated 6 months ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50Updated 5 months ago
- ☆13Updated 7 years ago
- Trigger the Google Genomics Pipeline API with CWL☆11Updated 8 years ago
- Nextflow workshop 2018 -- Training pages -> https://nextflow-io.github.io/nf-hack18/☆18Updated 6 years ago
- Import a CWL workflow specification to Nextflow script (experimental)☆27Updated 6 years ago
- Stupid Simple Structural Variant View☆25Updated 8 years ago
- Galaxy tools and workflows developed at the Earlham Institute☆14Updated 2 months ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago
- CheckQC inspects the content of an Illumina runfolder and determines if it passes a set of quality criteria☆28Updated last week
- A configurable de novo assembly pipeline☆28Updated 8 years ago
- Parallel merging, squaring off and ensemble calling for genomic variants☆20Updated 5 years ago
- Curated collection of open-source bioinformatics tools☆28Updated 6 years ago
- Request for comments on interchangeable bioinformatics containers☆40Updated 5 years ago
- An algorithm for clonal tree reconstruction from multi-sample cancer sequencing data☆14Updated 7 years ago
- Turn Galaxy Workflows into standalone scripts.☆9Updated 2 years ago
- What's The Function of these genes?☆22Updated 8 years ago
- CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.☆29Updated 4 years ago
- ☆37Updated 4 years ago
- robust matching of small variant datasets using flexible scoring schemes☆10Updated 5 years ago
- GenoTypes Compressor☆15Updated 3 years ago